1-Methyl-3-phenyl-1H-pyrazole-4-carbaldehyde

95%

Reagent Code: #214101
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CAS Number 304477-40-5

science Other reagents with same CAS 304477-40-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 186.213 g/mol
Formula C₁₁H₁₀N₂O
thermostat Physical Properties
Boiling Point 356.4±30.0 °C(Predicted)
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nonsteroidal anti-inflammatory drugs (NSAIDs) and selective COX-2 inhibitors. It serves as a building block in heterocyclic chemistry, enabling the construction of complex pyrazole derivatives with potential biological activity. Its aldehyde functional group allows for easy modification through condensation, reduction, or nucleophilic addition reactions, making it valuable in medicinal chemistry for generating compound libraries for drug screening. Also employed in agrochemical research for designing new pesticides and herbicides due to the bioactive nature of pyrazole scaffolds.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,630.00
inventory 250mg
10-20 days ฿9,150.00
inventory 1g
10-20 days ฿25,780.00

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1-Methyl-3-phenyl-1H-pyrazole-4-carbaldehyde
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nonsteroidal anti-inflammatory drugs (NSAIDs) and selective COX-2 inhibitors. It serves as a building block in heterocyclic chemistry, enabling the construction of complex pyrazole derivatives with potential biological activity. Its aldehyde functional group allows for easy modification through condensation, reduction, or nucleophilic addition reactions, making it valuable in medicinal chemistry for generat

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nonsteroidal anti-inflammatory drugs (NSAIDs) and selective COX-2 inhibitors. It serves as a building block in heterocyclic chemistry, enabling the construction of complex pyrazole derivatives with potential biological activity. Its aldehyde functional group allows for easy modification through condensation, reduction, or nucleophilic addition reactions, making it valuable in medicinal chemistry for generating compound libraries for drug screening. Also employed in agrochemical research for designing new pesticides and herbicides due to the bioactive nature of pyrazole scaffolds.

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